Cargando…
Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants
Transmission bottlenecks limit the spread of novel mutations and reduce the efficiency of selection along a transmission chain. While increased force of infection, receptor binding, or immune evasion may influence bottleneck size, the relationship between transmissibility and the transmission bottle...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844183/ https://www.ncbi.nlm.nih.gov/pubmed/36650162 http://dx.doi.org/10.1038/s41467-023-36001-5 |
_version_ | 1784870563148201984 |
---|---|
author | Bendall, Emily E. Callear, Amy P. Getz, Amy Goforth, Kendra Edwards, Drew Monto, Arnold S. Martin, Emily T. Lauring, Adam S. |
author_facet | Bendall, Emily E. Callear, Amy P. Getz, Amy Goforth, Kendra Edwards, Drew Monto, Arnold S. Martin, Emily T. Lauring, Adam S. |
author_sort | Bendall, Emily E. |
collection | PubMed |
description | Transmission bottlenecks limit the spread of novel mutations and reduce the efficiency of selection along a transmission chain. While increased force of infection, receptor binding, or immune evasion may influence bottleneck size, the relationship between transmissibility and the transmission bottleneck is unclear. Here we compare the transmission bottleneck of non-VOC SARS-CoV-2 lineages to those of Alpha, Delta, and Omicron. We sequenced viruses from 168 individuals in 65 households. Most virus populations had 0–1 single nucleotide variants (iSNV). From 64 transmission pairs with detectable iSNV, we identify a per clade bottleneck of 1 (95% CI 1–1) for Alpha, Delta, and Omicron and 2 (95% CI 2–2) for non-VOC. These tight bottlenecks reflect the low diversity at the time of transmission, which may be more pronounced in rapidly transmissible variants. Tight bottlenecks will limit the development of highly mutated VOC in transmission chains, adding to the evidence that selection over prolonged infections may drive their evolution. |
format | Online Article Text |
id | pubmed-9844183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98441832023-01-18 Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants Bendall, Emily E. Callear, Amy P. Getz, Amy Goforth, Kendra Edwards, Drew Monto, Arnold S. Martin, Emily T. Lauring, Adam S. Nat Commun Article Transmission bottlenecks limit the spread of novel mutations and reduce the efficiency of selection along a transmission chain. While increased force of infection, receptor binding, or immune evasion may influence bottleneck size, the relationship between transmissibility and the transmission bottleneck is unclear. Here we compare the transmission bottleneck of non-VOC SARS-CoV-2 lineages to those of Alpha, Delta, and Omicron. We sequenced viruses from 168 individuals in 65 households. Most virus populations had 0–1 single nucleotide variants (iSNV). From 64 transmission pairs with detectable iSNV, we identify a per clade bottleneck of 1 (95% CI 1–1) for Alpha, Delta, and Omicron and 2 (95% CI 2–2) for non-VOC. These tight bottlenecks reflect the low diversity at the time of transmission, which may be more pronounced in rapidly transmissible variants. Tight bottlenecks will limit the development of highly mutated VOC in transmission chains, adding to the evidence that selection over prolonged infections may drive their evolution. Nature Publishing Group UK 2023-01-17 /pmc/articles/PMC9844183/ /pubmed/36650162 http://dx.doi.org/10.1038/s41467-023-36001-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bendall, Emily E. Callear, Amy P. Getz, Amy Goforth, Kendra Edwards, Drew Monto, Arnold S. Martin, Emily T. Lauring, Adam S. Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants |
title | Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants |
title_full | Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants |
title_fullStr | Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants |
title_full_unstemmed | Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants |
title_short | Rapid transmission and tight bottlenecks constrain the evolution of highly transmissible SARS-CoV-2 variants |
title_sort | rapid transmission and tight bottlenecks constrain the evolution of highly transmissible sars-cov-2 variants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9844183/ https://www.ncbi.nlm.nih.gov/pubmed/36650162 http://dx.doi.org/10.1038/s41467-023-36001-5 |
work_keys_str_mv | AT bendallemilye rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT callearamyp rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT getzamy rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT goforthkendra rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT edwardsdrew rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT montoarnolds rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT martinemilyt rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants AT lauringadams rapidtransmissionandtightbottlenecksconstraintheevolutionofhighlytransmissiblesarscov2variants |